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Neurology|February 11, 2000
Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 geneG De Michele, A Filla, F Cavalcanti, et al.Neurology|January 14, 2004
A novel mutation in SACS gene in a family from southern ItalyC Criscuolo, S Banfi, M Orio, et al.Annals of Neurology|March 1, 1995
Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9qF Palau, G De Michele, J J Vilchez, et al.Journal of the Neurological Sciences|October 1, 1996
Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypesA Filla, G De Michele, G Campanella, et al.European Journal of Neurology|August 26, 2006
Long-term clinical experience with weekly interferon beta-1a in relapsing multiple sclerosisG Coppola, R Lanzillo, C Florio, et al.Neurology|November 26, 2003
Intergenerational instability and marked anticipation in SCA-17F Maltecca, A Filla, I Castaldo, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
Dementia, ataxia, extrapyramidal features, and epilepsy: phenotype spectrum in two Italian families with spinocerebellar ataxia type 17G De Michele, F Maltecca, M Carella, et al.Parkinsonism & Related Disorders|January 4, 2016
Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonismA De Rosa, T Pellegrino, S Pappatà, et al.Journal of Medical Genetics|June 6, 2008
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonismC Piccoli, M Ripoli, G Quarato, et al.Journal of Neurology|July 10, 1999
Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular studyG Coppola, G De Michele, F Cavalcanti, et al.Pageof 13